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A feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint
We perform logic-based network analysis on a model of the mammalian cell cycle. This model is composed of a Restriction Switch driving cell cycle commitment and a Phase Switch driving mitotic entry and exit. By generalizing the concept of stable motif, i.e., a self-sustaining positive feedback loop...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848090/ https://www.ncbi.nlm.nih.gov/pubmed/31712566 http://dx.doi.org/10.1038/s41598-019-52725-1 |
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author | Deritei, Dávid Rozum, Jordan Ravasz Regan, Erzsébet Albert, Réka |
author_facet | Deritei, Dávid Rozum, Jordan Ravasz Regan, Erzsébet Albert, Réka |
author_sort | Deritei, Dávid |
collection | PubMed |
description | We perform logic-based network analysis on a model of the mammalian cell cycle. This model is composed of a Restriction Switch driving cell cycle commitment and a Phase Switch driving mitotic entry and exit. By generalizing the concept of stable motif, i.e., a self-sustaining positive feedback loop that maintains an associated state, we introduce the concept of a conditionally stable motif, the stability of which is contingent on external conditions. We show that the stable motifs of the Phase Switch are contingent on the state of three nodes through which it receives input from the rest of the network. Biologically, these conditions correspond to cell cycle checkpoints. Holding these nodes locked (akin to a checkpoint-free cell) transforms the Phase Switch into an autonomous oscillator that robustly toggles through the cell cycle phases G1, G2 and mitosis. The conditionally stable motifs of the Phase Switch Oscillator are organized into an ordered sequence, such that they serially stabilize each other but also cause their own destabilization. Along the way they channel the dynamics of the module onto a narrow path in state space, lending robustness to the oscillation. Self-destabilizing conditionally stable motifs suggest a general negative feedback mechanism leading to sustained oscillations. |
format | Online Article Text |
id | pubmed-6848090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68480902019-11-19 A feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint Deritei, Dávid Rozum, Jordan Ravasz Regan, Erzsébet Albert, Réka Sci Rep Article We perform logic-based network analysis on a model of the mammalian cell cycle. This model is composed of a Restriction Switch driving cell cycle commitment and a Phase Switch driving mitotic entry and exit. By generalizing the concept of stable motif, i.e., a self-sustaining positive feedback loop that maintains an associated state, we introduce the concept of a conditionally stable motif, the stability of which is contingent on external conditions. We show that the stable motifs of the Phase Switch are contingent on the state of three nodes through which it receives input from the rest of the network. Biologically, these conditions correspond to cell cycle checkpoints. Holding these nodes locked (akin to a checkpoint-free cell) transforms the Phase Switch into an autonomous oscillator that robustly toggles through the cell cycle phases G1, G2 and mitosis. The conditionally stable motifs of the Phase Switch Oscillator are organized into an ordered sequence, such that they serially stabilize each other but also cause their own destabilization. Along the way they channel the dynamics of the module onto a narrow path in state space, lending robustness to the oscillation. Self-destabilizing conditionally stable motifs suggest a general negative feedback mechanism leading to sustained oscillations. Nature Publishing Group UK 2019-11-11 /pmc/articles/PMC6848090/ /pubmed/31712566 http://dx.doi.org/10.1038/s41598-019-52725-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Deritei, Dávid Rozum, Jordan Ravasz Regan, Erzsébet Albert, Réka A feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint |
title | A feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint |
title_full | A feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint |
title_fullStr | A feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint |
title_full_unstemmed | A feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint |
title_short | A feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint |
title_sort | feedback loop of conditionally stable circuits drives the cell cycle from checkpoint to checkpoint |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848090/ https://www.ncbi.nlm.nih.gov/pubmed/31712566 http://dx.doi.org/10.1038/s41598-019-52725-1 |
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